🇺🇸
United States · US · US:68084-204_43e0ff0a-c0e4-97fc-e063-6294a90ae3dd
Minoxidil
Orange BookUNIISPLATC C02DC01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmerican Health Packaging
CountryUS (United States)
ATC codeC02DC01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116808420401100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-204-01) / 1 TABLET in 1 BLISTER PACK (68084-204-11)
Annotations
UNII (FDA Substance ID)
5965120SH1
MINOXIDIL
RxCUI 6984
Orange Book
A071826
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5965120SH1",
"rxcui": "6984",
"inchikey": "ZFMITUMMTDLWHR-UHFFFAOYSA-N",
"display_name": "MINOXIDIL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"1b54eca8-4a96-1b5e-e063-6394a90a7b94": {
"match": "brand_token",
"title": "MINOXIDIL (MINOXIDIL FOAM 5% (WOMENS)) AEROSOL, FOAM [CLARITY COSMETICS INC.]",
"spl_version": "2",
"published_date": "2026-06-02"
}
},
"productid": "68084-204_43e0ff0a-c0e4-97fc-e063-6294a90ae3dd",
"productndc": "68084-204",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "071826",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "2.5MG",
"product_no": "001",
"approval_date": "Nov 14, 1988"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MINOXIDIL",
"proprietary_name": "Minoxidil",
"active_ingred_unit": "mg/1",
"application_number": "ANDA071826",
"marketing_category": "ANDA",
"nonproprietary_name": "Minoxidil",
"start_marketing_date": "20070910",
"active_numerator_strength": "2.5"
}Related drugs
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